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HEXADECYL ACRYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13402-02-3 Structure
  • Basic information

    1. Product Name: HEXADECYL ACRYLATE
    2. Synonyms: 2-Propenoicacid,hexadecylester;ACRYLIC ACID HEXADECYL ESTER;HEXADECYL ACRYLATE;Hexadecylacrylat;Hexadecyl Acrylate (stabilized with MEHQ);Acrylic acid cetyl ester;Hexadecyl acrylatae;Hexadecyl Acrylate 
    3. CAS NO:13402-02-3
    4. Molecular Formula: C19H36O2
    5. Molecular Weight: 296.49
    6. EINECS: 236-492-0
    7. Product Categories: monomer
    8. Mol File: 13402-02-3.mol
  • Chemical Properties

    1. Melting Point: 24 °C
    2. Boiling Point: 170°C 15mm
    3. Flash Point: 178 °C
    4. Appearance: /
    5. Density: 0.87
    6. Vapor Pressure: 1.1E-05mmHg at 25°C
    7. Refractive Index: 1.4480-1.4520
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. Water Solubility: 1.194μg/L at 25℃
    11. CAS DataBase Reference: HEXADECYL ACRYLATE(CAS DataBase Reference)
    12. NIST Chemistry Reference: HEXADECYL ACRYLATE(13402-02-3)
    13. EPA Substance Registry System: HEXADECYL ACRYLATE(13402-02-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 13402-02-3(Hazardous Substances Data)

13402-02-3 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 13402-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,0 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13402-02:
(7*1)+(6*3)+(5*4)+(4*0)+(3*2)+(2*0)+(1*2)=53
53 % 10 = 3
So 13402-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H36O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-21-19(20)4-2/h4H,2-3,5-18H2,1H3

13402-02-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name hexadecyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names Pamityl acrylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13402-02-3 SDS

13402-02-3Downstream Products

13402-02-3Relevant articles and documents

Synthesis and Surface Properties of a Novel Sodium 3-(3-Alkyloxy-3-oxopropoxy)-3-oxopropane-1-sulfonate at the Air-Water Interface

Kumar, Pandari Phani,Nayak, Rati Ranjan,Kanjilal, Sanjit

, p. 689 - 695 (2015)

The present paper describes the synthesis and evaluation of surface properties of a novel series of anionic surfactant, namely sodium 3-(3-alkyloxy-3-oxopropoxy)-3-oxopropane-1-sulfonate with varying alkyl chain length (C8-C16). Synthesis involves initial formation of the 3-alkyloxy-3-oxopropyl acrylate along with fatty acrylate during the direct esterification of fatty alcohol with acrylic acid in the presence of 0.5 % NaHSO4 at 110 C followed by sulfonation of the terminal double bond of the 3-alkyloxy-3-oxopropyl acrylate. Synthesized compounds were evaluated for surface and thermodynamic properties such as critical micelle concentration (CMC), surface tension at CMC (γcmc), efficiency of surface adsorption (pC20), surface excess (Γmax), minimum area per molecule at the air-water interface (A min), free energy of adsorption (?G ads), free energy of micellization (?G mic), wetting time, emulsifying properties, foaming power and calcium tolerance. Effect of chain length on CMC follows the classic trend, i.e. decrease in CMC with the increase in alkyl chain length. High pC20 (>3) value indicates higher hydrophobic character of the surfactant. These surfactants showed very poor wetting time and calcium tolerance, but exhibited good emulsion stability and excellent foamability. Foaming power and foam stability of C14-sulfonate were found to be the best among the studied compounds. Foam stability of C14-sulfonate was also studied at different concentrations over time and excellent foam stability was obtained at a concentration of 0.075 %. Thus this novel class of surfactant may find applications as foam boosters in combination with other suitable surfactants.

Non-Viral CRISPR/Cas Gene Editing In Vitro and In Vivo Enabled by Synthetic Nanoparticle Co-Delivery of Cas9 mRNA and sgRNA

Miller, Jason B.,Zhang, Shuyuan,Kos, Petra,Xiong, Hu,Zhou, Kejin,Perelman, Sofya S.,Zhu, Hao,Siegwart, Daniel J.

, p. 1059 - 1063 (2017)

CRISPR/Cas is a revolutionary gene editing technology with wide-ranging utility. The safe, non-viral delivery of CRISPR/Cas components would greatly improve future therapeutic utility. We report the synthesis and development of zwitterionic amino lipids (ZALs) that are uniquely able to (co)deliver long RNAs including Cas9 mRNA and sgRNAs. ZAL nanoparticle (ZNP) delivery of low sgRNA doses (15 nm) reduces protein expression by >90 % in cells. In contrast to transient therapies (such as RNAi), we show that ZNP delivery of sgRNA enables permanent DNA editing with an indefinitely sustained 95 % decrease in protein expression. ZNP delivery of mRNA results in high protein expression at low doses in vitro (?1). Intravenous co-delivery of Cas9 mRNA and sgLoxP induced expression of floxed tdTomato in the liver, kidneys, and lungs of engineered mice. ZNPs provide a chemical guide for rational design of long RNA carriers, and represent a promising step towards improving the safety and utility of gene editing.

Synthesis of lipophilic 1-substituted diazen-1-IUM-1,2-diolates

Roselle, Dominick C.,Smith, Daniel J.

, p. 747 - 749 (1997)

A new class of 1-substituted diazen-1-ium-1,2-diolates (nitric oxide donors previously known as NONOates) were obtained by preparing esters of the naturally occurring polyamines putreanine (1) and spermic acid (2) with either cholesterol or hexadecanol. T

Preparation method for synthesizing high-carbon alkyl acrylate through catalyzing in-situ acid resin

-

Paragraph 0044; 0045, (2018/11/27)

The invention belongs to the technical field of organic synthesis and in particular relates to a preparation method for synthesizing high-carbon alkyl acrylate through catalyzing in-situ acid resin. The preparation method comprises the following steps: mixing acrylic acid, the in-situ acid resin, acrylic high-carbon alkyl alcohol, hydroquinone and cyclohexane according to a certain ratio; stirringand heating, and controlling reaction time; after reaction is finished, filtering to remove a resin catalyst; carrying out water washing, neutralization and water washing to obtain the high-carbon alkyl acrylate. According the preparation method provided by the invention, the yield of high-carbon alkyl acrylate can be improved; the in-situ acid resin can be repeatedly utilized, resources are saved and the environment is protected.

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